ClinVar Miner

Submissions for variant NM_007298.3(BRCA1):c.788-1790T>A (rs1555589094)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000585811 SCV000693743 pathogenic FANCONI ANEMIA, COMPLEMENTATION GROUP S 2019-04-16 no assertion criteria provided literature only
OMIM RCV000585837 SCV000693744 pathogenic Breast-ovarian cancer, familial 1 2019-04-16 no assertion criteria provided literature only

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